Changes in haemostatic parameters during the menstrual cycle and subsequent use of drospirenone-containing oral contraceptives

Thromb Res. 2014 Nov;134(5):1032-7. doi: 10.1016/j.thromres.2014.09.008. Epub 2014 Sep 16.

Abstract

Introduction: Oral contraceptives (OC) increase the risk of venous thromboembolism that depends on the OC formulation and could at least partially be explained by impaired function of the protein C-system (APC resistance) and the tissue factor pathway inhibitor (TFPI)-system. There is limited information available on the effects of OC, containing a newer progestogen- drospirenone (DRSP-OC) on these two major anticoagulant pathways, thrombin generation, reflecting the overall state of coagulation, and other coagulation parameters.

Methods: In a study population consisting of 14 healthy women (age 21-33 years) we investigated the effect of the menstrual cycle and subsequent use of DRSP-OC on APC resistance, the function of the TFPI-system, thrombin generation and on their major determinants, i.e. prothrombin, antithrombin, FV, FX, FVIII, protein C, protein S(total and free) and TFPI(full-length and free).

Results: All studied parameters remained unchanged during the menstrual cycle. During DRSP-OC use we observed a significant increase in APC resistance (~2.4-fold), thrombin generation measured at low (~2.2-fold) and high tissue factor concentrations (~1.4-fold), plasma concentrations of prothrombin (19%), FX (31%), FVIII (17%) and protein C (43%). DRSP-OC use impaired the function of the TFPI-system and decreased plasma levels of antithrombin (-6%), FV (-22%), protein Stotal (-21%), protein Sfree (-20%), TFPIfull-length (-36%) and TFPIfree (-46%).

Conclusions: DRSP-OC caused procoagulant changes in all studied haemostatic parameters. The impairment of the protein C- and TFPI-systems was more pronounced than the impairment of the coagulation pathways and can at least partially account for the increased risk of venous thromboembolism in users of DRSP-OC.

Keywords: Drospirenone-containing oral contraceptives; Protein S; TFPI; Tthrombin generation.

MeSH terms

  • Adult
  • Androstenes / pharmacology*
  • Blood Coagulation / drug effects
  • Contraceptives, Oral / pharmacology*
  • Female
  • Hemostasis / drug effects*
  • Humans
  • Lipoproteins / metabolism
  • Menstrual Cycle
  • Protein S / metabolism
  • Thrombin / metabolism
  • Young Adult

Substances

  • Androstenes
  • Contraceptives, Oral
  • Lipoproteins
  • Protein S
  • lipoprotein-associated coagulation inhibitor
  • Thrombin
  • drospirenone